510(k) K921795
K921795 is an FDA 510(k) premarket notification submitted by Bacton Assay Systems, Inc. for the device "BACTON(TM), AUTO-APO A-1 REAGENT". The FDA issued a decision of Substantially Equivalent on June 23, 1992. The device falls under product code MSJ (Apolipoproteins), a Class I device regulated under 21 CFR 862.1475. Bacton Assay Systems, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 23, 1992
- Date Received
- April 10, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Apolipoproteins
- Device Class
- Class I
- Regulation Number
- 862.1475
- Review Panel
- CH
- Submission Type